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Long-term follow-up of an 8-year-old boy with insulinoma as the first manifestation of a familial form of multiple endocrine neoplasia type 1.
Fabbri HC, Mello MP, Soardi FC, Esquiaveto-Aun AM, Oliveira DM, Denardi FC, Moura-Neto A, Garmes HM, Baptista MT, Matos PS, Lemos-Marini SH, D'Souza-Li LF, Guerra-Júnior G. Fabbri HC, et al. Among authors: denardi fc. Arq Bras Endocrinol Metabol. 2010 Nov;54(8):754-60. doi: 10.1590/s0004-27302010000800016. Arq Bras Endocrinol Metabol. 2010. PMID: 21340165
Six new cases confirm the clinical molecular profile of complete combined 17α-hydroxylase/ 17,20-lyase deficiency in Brazil.
Belgini DR, Mello MP, Baptista MT, Oliveira DM, Denardi FC, Garmes HM, Grassiotto Oda R, Benetti Pinto CL, Marques-de-Faria AP, Maciel-Guerra AT, Guerra-Júnior G. Belgini DR, et al. Among authors: denardi fc. Arq Bras Endocrinol Metabol. 2010 Nov;54(8):711-6. doi: 10.1590/s0004-27302010000800008. Arq Bras Endocrinol Metabol. 2010. PMID: 21340157
Orbital lymphoma mimicking ophthalmopathy in a patient with Graves'.
Moura Neto A, Denardi FC, Delamain MT, Tambascia MA, Vassallo J, Caldato R, Zantut-Wittmann DE. Moura Neto A, et al. Among authors: denardi fc. Am J Med Sci. 2012 Nov;344(5):418-21. doi: 10.1097/MAJ.0b013e3182582330. Am J Med Sci. 2012. PMID: 22885624